Zobrazeno 1 - 6
of 6
pro vyhledávání: '"David A. F. Langnel"'
Publikováno v:
ARKIVOC, Vol 2000, Iss 3, Pp 421-437 (2000)
Externí odkaz:
https://doaj.org/article/21ab0a02507744379c40e1ff37c40a50
Publikováno v:
ARKIVOC, Vol 2000, Iss 3, Pp 421-437 (2000)
The imidazo(5,1-d)-1,2,3,5-tetrazine ring-system is hypersensitive to attack by nucleophiles. Therefore, acidic conditions were applied successfully to synthesise new 8-substituted derivatives of the antitumor agents temozolomide (1a) and mitozolomid
Autor:
Jill Arrowsmith, Malcolm F. G. Stevens, David A. F. Langnel, Richard T. Wheelhouse, Sharon A. Jennings
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :4432-4438
Bis(imidazotetrazine)s (16), related in structure to the antitumour agents mitozolomide (1a) and temozolomide (1b), but linked through the N(3)–N(3′) atoms of the imidazo[5,1-d][1,2,3,5]tetrazine ring-systems, are prepared by interaction of 5-dia
Autor:
David A. F. Langnel, Yongfeng Wang, Malcolm F. G. Stevens, Linxiang Zhao, Richard T. Wheelhouse
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1669-1676
Novel 3-substituted imidazo[5,1-d][1,2,3,5]tetrazinones 3 have been prepared by two routes: reaction of 5-diazoimidazole-4-carboxamide 2 and isocyanates, and nitrosative cyclisation of 5-amino-1-carbamoylimidazole-4-carboxamides 7. The latter cyclisa
Publikováno v:
ChemInform. 29
Autor:
David A. F. Langnel, Jill Arrowsmith, Malcolm F. G. Stevens, Sharon A. Jennings, Richard T. Wheelhouse
Publikováno v:
ChemInform. 32